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FDA 510(k)

KIDD VAGINAL SPECULUM

K-Number: K841867 · 1984-07-13

ApplicantPaul H. Schneider Ent.
Decision Date1984-07-13
Product CodeHIB
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

KIDD VAGINAL SPECULUM is the device name listed in this FDA 510(k) record. The listed applicant is Paul H. Schneider Ent.. It received FDA 510(k) clearance on 1984-07-13 under 510(k) number K841867. The device is classified under product code HIB. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KIDD VAGINAL SPECULUM?

KIDD VAGINAL SPECULUM is a medical device that received FDA 510(k) clearance on 1984-07-13. The listed applicant is Paul H. Schneider Ent.. The 510(k) number is K841867.

When did KIDD VAGINAL SPECULUM receive FDA 510(k) clearance?

KIDD VAGINAL SPECULUM received FDA 510(k) clearance on 1984-07-13, under 510(k) number K841867.

Who is the listed applicant for KIDD VAGINAL SPECULUM?

The FDA 510(k) record lists Paul H. Schneider Ent. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KIDD VAGINAL SPECULUM?

The FDA product code for KIDD VAGINAL SPECULUM is HIB.

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Related Devices (Code: HIB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K252208JFord Speculum Sleeve™Ford Medtech, LLCK130046CLEARSPEC SINGLE USE VAGINAL SPECULUMClearspec, LLCK120743SPECULUM, VAGINAL, NONMETALWelch Allyn, Inc.K110766KOLPLUX SYSTEMKolplast CI LtdaK092870NON-STERILE DISPOSABLE VAGINAL SPECULUMKunshan Deyi Plastic Co., Ltd.K091937OFFICE-SPEC DISPOSABLE SIDE-OPENING SPECULUMObp Corporation

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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